Tri Dental Implants Int. AG is one of 92 FDA 510(k) medical device manufacturers from Switzerland in the dataset, ranked by real submission volume.
Tri Dental Implants Int. AG - FDA 510(k) Cleared Devices
Recent clearances: TRI-matrix® X-Force Implants, TRI-matrix Implant Line
3
Total
3
Cleared
0
Denied
Tri Dental Implants Int. AG has 3 FDA 510(k) cleared medical devices. Based in Baar, CH.
Latest FDA clearance: Jan 2025. Active since 2015. Primary specialty: Dental.
Browse the FDA 510(k) cleared devices submitted by Tri Dental Implants Int. AG Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by PaxMed International, LLC as regulatory consultant.
FDA 510(k) Regulatory Record - Tri Dental Implants Int. AG
3 devices